CAS 2226-96-2
:templo
Descrição:
templo, com o número CAS 2226-96-2, é um radical nitroxilo estável que é frequentemente utilizado em pesquisas bioquímicas e farmacológicas. É caracterizado por sua capacidade de atuar como um captador de radicais livres, o que o torna valioso em estudos relacionados ao estresse oxidativo e danos celulares. templo possui propriedades antioxidantes, ajudando a neutralizar espécies reativas de oxigênio (ROS) prejudiciais em sistemas biológicos. Este composto é tipicamente solúvel em água e solventes orgânicos, permitindo aplicações versáteis em várias condições experimentais. Além disso, templo tem sido investigado por seus potenciais efeitos terapêuticos em condições como doenças cardiovasculares, distúrbios neurodegenerativos e inflamação. Sua estabilidade e reatividade o tornam uma ferramenta útil para entender a biologia redox e os mecanismos de dano oxidativo. No geral, templo serve como um composto importante tanto na pesquisa quanto em potenciais aplicações clínicas devido às suas propriedades químicas únicas e significado biológico.
Fórmula:C9H18NO2
InChI:InChI=1S/C9H18NO2/c1-8(2)5-7(11)6-9(3,4)10(8)12/h7,11H,5-6H2,1-4H3
Chave InChI:InChIKey=UZFMOKQJFYMBGY-UHFFFAOYSA-N
SMILES:CC1(C)CC(CC(C)(C)N1O)O
Sinónimos:- (4-Hydroxy-2,2,6,6-Tetramethylpiperidin-1-Yl)Oxidanyl
- 1-Oxyl-2,2,6,6-tetramethyl-4-hydroxypiperidine
- 1-Oxyl-2,2,6,6-tetramethyl-4-piperidinol
- 1-Piperidinyloxy, 4-hydroxy-2,2,6,6-tetramethyl-
- 2,2,6,6-Tetramethyl-1-oxy-4-hydroxypiperidine
- 2,2,6,6-Tetramethyl-4-hydroxy-1-piperidinyloxy radical
- 2,2,6,6-Tetramethyl-4-hydroxylpiperidine-1-oxyl
- 2,2,6,6-Tetramethyl-4-hydroxypiperidin-1-oxyl
- 2,2,6,6-Tetramethyl-4-hydroxypiperidine 1-oxide radical
- 2,2,6,6-Tetramethyl-4-hydroxypiperidine N-oxide
- 2,2,6,6-Tetramethyl-4-hydroxypiperidine oxide
- 2,2,6,6-Tetramethyl-4-hydroxypiperidine-1-hydroxyl
- 2,2,6,6-Tetramethyl-4-hydroxypiperidine-1-oxyl
- 2,2,6,6-Tetramethyl-4-hydroxypiperidine-1-oxyl radical
- 2,2,6,6-Tetramethyl-4-hydroxypiperidinooxy
- 2,2,6,6-Tetramethyl-4-hydroxypiperidinooxy radical
- 2,2,6,6-Tetramethyl-4-hydroxypiperidinyl-1-oxy
- 2,2,6,6-Tetramethyl-4-hydroxypiperidinyl-1-oxyl
- 2,2,6,6-Tetramethyl-4-hydroxypiperidinyloxy radical
- 2,2,6,6-Tetramethyl-4-hydroxypiperidinyloxyl radical
- 2,2,6,6-Tetramethyl-4-hydroxypiperidyl 1-oxyl
- 2,2,6,6-Tetramethyl-4-oxypiperidine-1-oxyl
- 2,2,6,6-Tetramethyl-4-piperidinol 1-oxide
- 2,2,6,6-Tetramethyl-4-piperidinol 1-oxyl
- 2,2,6,6-Tetramethyl-4-piperidinol N-oxyl
- 2,2,6,6-Tetramethyl-4-piperidinol nitroxide
- 2,2,6,6-Tetramethyl-4-piperidinol-1-oxy
- 2,2,6,6-Tetramethyl-4-piperidinol-1-oxyl radical
- 2,2,6,6-Tetramethylpiperidine-4-hydroxy-1-oxyl
- 2,2,6,6-Tetramethylpiperidine-N-oxyl-4-ol
- 2,2,6,6-Tetramethylpiperidinol-4-oxyl-1
- 2.2.6.6-Tetramethyl-Freeagaoxy-4-Piperidyl
- 4-Hidroxi-2,2,6,6-Tetrametilpiperidinoxil
- 4-Ho-Tempo
- 4-Hydroxy-1-oxyl-2,2,6,6-tetramethylpiperidine
- 4-Hydroxy-2,2,6,6-Tetramethylpiperidinoxyl
- 4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinoxy
- 4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinoxyl
- 4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy
- 4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy radical
- 4-Hydroxy-2,2,6,6-tetramethyl-piperidinyloxy
- 4-Hydroxy-2,2,6,6-tetramethylpiperidine 1-oxide radical
- 4-Hydroxy-2,2,6,6-tetramethylpiperidine N-oxide
- 4-Hydroxy-2,2,6,6-tetramethylpiperidine oxide
- 4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl
- 4-Hydroxy-2,2,6,6-tetramethylpiperidine-N-oxy
- 4-Hydroxy-2,2,6,6-tetramethylpiperidine-N-oxyl
- 4-Hydroxy-2,2,6,6-tetramethylpiperidino-1-oxyl
- 4-Hydroxy-2,2,6,6-tetramethylpiperidinooxy
- 4-Hydroxy-2,2,6,6-tetramethylpiperidinooxy radical
- 4-Hydroxy-2,2,6,6-tetramethylpiperidinoxy
- 4-Hydroxy-2,2,6,6-tetramethylpiperidinoxyle
- 4-Hydroxy-2,2,6,6-tetramethylpiperidinyl-1-oxyl
- 4-Hydroxy-2,2,6,6-tetramethylpiperidinyl-N-oxy
- 4-Hydroxy-2,2,6,6-tetramethylpiperidinyl-N-oxyl
- 4-Hydroxy-2,2,6,6-tetramethylpiperidinyloxy
- 4-Hydroxy-2,2,6,6-tetramethylpiperidinyloxyl
- 4-Hydroxy-2,2,6,6-tetramethylpiperidyl-1-oxyl
- 4-Hydroxy-2,6-Tetramethyl-Piperidine-1-Oxide
- 4-Hydroxy-TEMPO
- 4-OH-Tempo
- 4-Oxypiperidol
- 4-hydroxyl-2,2,6,6-tetramethylpiperidine-1-Oxyl
- 4H-Tempo
- ADK Stab LA 7RD
- ADK Stab NA 7RD
- H 0865
- H-Tempo
- Hotempo
- Htempo
- HyTEMPO
- In701
- La 7Rd
- Nitroxyl 2
- Nr I
- Petroflo 20Y104
- Piperidine, 4-Hydroxy-2,2,6,6-Tetramethyl-1-Oxy-
- Piperidinooxy, 4-hydroxy-2,2,6,6-tetramethyl-
- Polystast 7200P
- Polystop 7010
- Polystop 7300P
- Prostab 5198
- Spj 701
- Tanol
- Tempo OH
- Tempol
- Tempole
- Tetramethyl-2,2,6,6-aza-1-cyclohexanol-4-oxide-1
- Tmhpo
- Tmpn
- Uv-1198
- Zj 01
- Zj 705
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4-Hydroxy-2,2,6,6-tetramethylpiperidine 1-Oxyl Free Radical
CAS:Fórmula:C9H18NO2Pureza:>98.0%(GC)Cor e Forma:Light yellow to Brown powder to lumpPeso molecular:172.254-Hydroxy-TEMPO, free radical, 98+%
CAS:Superoxide scavenger with neuroprotective, anti-inflammatory and analgesic effects4-Hydroxy-TEMPO free radical is used as a catalyst and a chemical oxidant by virtue of being a stable radical. It is used for detoxifying reactive oxygen species in medicinal chemistry. It is involved in the catalysisFórmula:C9H18NO2Pureza:98+%Cor e Forma:Crystals or powder or crystalline powder or flakes, OrangePeso molecular:172.254-Hydroxy TEMPO, free radical
CAS:Fórmula:C9H18NO2Pureza:(GC) ≥ 98%Cor e Forma:Yellow to orange-red crystalline powder or solidPeso molecular:172.254-Hydroxy-2,2,6,6-tetramethyl-piperidine-d17-1-15N-1-oxyl"Carboglace"
CAS:Pureza:97 atom % D; 99 atom % 15NCor e Forma:Yellow-Orange SolidPeso molecular:190.364-Hydroxy-2,2,6,6-tetramethyl-piperidine-d17-1-oxyl"Carboglace"
CAS:Pureza:97 atom % DCor e Forma:Yellow-Orange SolidPeso molecular:189.354-Hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy
CAS:Fórmula:C9H18NO2Pureza:98%Cor e Forma:SolidPeso molecular:172.2447Ref: IN-DA00342N
25gA consultar200kgA consultar50g20,00€100g24,00€250g28,00€500g41,00€1kg53,00€5kg135,00€10kg218,00€25kg536,00€4-Hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy
CAS:Produto ControladoApplications A free radical scavenger; may be used for prophylaxis and treatment of IRI.
References Flather, M., et al.: Lancet, 355, 1575 (2000), Sasso, F., et al.: Metabolism, 52, 675 (2003), Kass, D., et al.: Circ. Res., 94, 1533 (2004), Murdoch, C., et al.: Cardiovasc Res., 71, 208 (2006),Fórmula:C9H18NO2Cor e Forma:NeatPeso molecular:172.244-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl
CAS:4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxylFórmula:C9H18NO2Pureza:>98%Cor e Forma:SolidPeso molecular:172.24471Tempol
CAS:Tempol (Tanol) is a superoxide scavenger. It has anti-inflammatory, neuroprotective and analgesic effects.Fórmula:C9H18NO2Pureza:97% - 99.98%Cor e Forma:Yellow SolidPeso molecular:172.254-Hydroxy-2,2,6,6-tetramethyl piperidinyloxy free radical
CAS:Fórmula:C9H18NO2Pureza:98%Cor e Forma:SolidPeso molecular:172.248Tempol
CAS:2,2,6,6-Tetramethyl-4-hydroxy-1-piperidinyloxy radicalFórmula:C9H18NO2Pureza:95%Peso molecular:172.242,2,6,6-Tetramethyl-4-piperidinol 1-oxyl, free radical
CAS:2,2,6,6-Tetramethyl-4-piperidinol 1-oxyl (TEMPO) is a reactive oxygen species that belongs to the group of nitroxide radicals. It can be used as a radical scavenger and has been shown to inhibit the production of pro-apoptotic proteins in human macrophages. TEMPO has also been shown to bind to DNA and prevent the binding of HIV viral protein gp120. TEMPO can be used as an inhibitor for glycol ethers in laboratory experiments. The most common use is as a water vapor scavenger during polymerization reactions in organic chemistry.Fórmula:C9H18NO2Pureza:Min. 98 Area-%Cor e Forma:Orange SolidPeso molecular:172.24 g/mol
